344748-71-6
1H-Indole, 4-ethyl-
CAS: 344748-71-6
Molecular Formula: C10H11N
344748-71-6 - Names and Identifiers
| Name | 1H-Indole, 4-ethyl- |
| Synonyms | 4-ethyl-1H-indole 1H-Indole, 4-ethyl- |
| CAS | 344748-71-6 |
344748-71-6 - Physico-chemical Properties
| Molecular Formula | C10H11N |
| Molar Mass | 145.2 |
344748-71-6 - Introduction
1H-Indole, 4-ethyl-is an organic compound with the chemical formula C10H11N. It is a derivative of indole in which the ethyl group is attached at position 4 of the indole.
1H-Indole, 4-ethyl-has the appearance of a light yellow solid and can be dissolved in organic solvents such as ethanol and dimethyl sulfoxide. It has a strong aromatic smell.
In practical applications, 1H-Indole, 4-ethyl-are often used as intermediates in organic synthesis. It can participate in a variety of reactions, such as aromatization reaction, olefin addition reaction and cyclization reaction. In addition, 1H-Indole, 4-ethyl-can also be used as a starting material in the synthesis of dyes, fluorescent probes and drugs.
1H-Indole, 4-ethyl-can be prepared in a variety of ways. One common method is by reacting an indole with an ethyl halide under basic conditions. In addition, other synthetic routes, such as oxidation, amination and reduction, may also be utilized.
Regarding safety information, due to individual differences, please follow the corresponding safety procedures and laboratory guidelines when using or operating 1H-Indole, 4-ethyl. It may be irritating to the skin, eyes and respiratory system, so appropriate protective equipment such as gloves, goggles and respiratory protection must be worn. Avoid contact with oxidizing agents and high temperatures during storage and handling. If accidentally inhaled or ingested, seek medical help immediately.
1H-Indole, 4-ethyl-has the appearance of a light yellow solid and can be dissolved in organic solvents such as ethanol and dimethyl sulfoxide. It has a strong aromatic smell.
In practical applications, 1H-Indole, 4-ethyl-are often used as intermediates in organic synthesis. It can participate in a variety of reactions, such as aromatization reaction, olefin addition reaction and cyclization reaction. In addition, 1H-Indole, 4-ethyl-can also be used as a starting material in the synthesis of dyes, fluorescent probes and drugs.
1H-Indole, 4-ethyl-can be prepared in a variety of ways. One common method is by reacting an indole with an ethyl halide under basic conditions. In addition, other synthetic routes, such as oxidation, amination and reduction, may also be utilized.
Regarding safety information, due to individual differences, please follow the corresponding safety procedures and laboratory guidelines when using or operating 1H-Indole, 4-ethyl. It may be irritating to the skin, eyes and respiratory system, so appropriate protective equipment such as gloves, goggles and respiratory protection must be worn. Avoid contact with oxidizing agents and high temperatures during storage and handling. If accidentally inhaled or ingested, seek medical help immediately.
Last Update：2024-04-09 21:04:16
